Home Cart Sign in  
Chemical Structure| 1135-32-6 Chemical Structure| 1135-32-6

Structure of 1135-32-6

Chemical Structure| 1135-32-6

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 1135-32-6 ]

CAS No. :1135-32-6
Formula : C12H10N2
M.W : 182.22
SMILES Code : C1(/C=C/C2=CC=NC=C2)=CC=NC=C1
InChI Key :MGFJDEHFNMWYBD-OWOJBTEDSA-N
Pubchem ID :776222

Safety of [ 1135-32-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 1135-32-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1135-32-6 ]

[ 1135-32-6 ] Synthesis Path-Downstream   1~11

  • 1
  • iron(II) nitrate [ No CAS ]
  • [ 7732-18-5 ]
  • [ 68-04-2 ]
  • [ 1135-32-6 ]
  • [Fe2(citrate)2(H2O)2][1,2-bis(4-pyridyl)ethene(+2H)] [ No CAS ]
  • 2
  • zinc(II) nitrate hexahydrate [ No CAS ]
  • [ 610-09-3 ]
  • [ 1135-32-6 ]
  • [Zn2(μ-e,a-cis-1,2-cyclohexanedicarboxylate)2(μ-1,2-bis(4-pyridyl)ethylene)]*2H2O [ No CAS ]
  • 3
  • cadmium(II) nitrate hexahydrate [ No CAS ]
  • [ 610-09-3 ]
  • [ 1135-32-6 ]
  • [ 1309059-90-2 ]
  • 4
  • [ 499-49-0 ]
  • [ 6046-93-1 ]
  • [ 1135-32-6 ]
  • Cu2(5-methylisophthalic acid(2-))2(1,2-di(4-pyridyl)-ethylene) [ No CAS ]
  • 5
  • cobalt(II) nitrate hexahydrate [ No CAS ]
  • [ 68-12-2 ]
  • [ 130-85-8 ]
  • [ 1135-32-6 ]
  • Co(2+)*2H2O*C12H10N2*C23H14O6(2-)*C3H7NO [ No CAS ]
YieldReaction ConditionsOperation in experiment
47% In water; N,N-dimethyl-formamide; at 120℃; for 60h;Autoclave; A mixture of Co(NO3)2¢6H2O (0.058 g, 0.2 mmol), H2pam (0.060 g, 0.2 mmol), bpa (0.036 g, 0.2 mmol), DMF (2 mL),and H2O (2 mL) was placed in a Parr Teflon-lined stainless steel vessel (23 mL). Then the vessel was sealed and heated to120C, and held for 60 h. Then the reactant mixture was cooled at a rate of 0.5C/min to lead to the formation of crystal 1. Yield: 47percent based on H2pam. Elemental Anal. Calcd.for C38H33CoN3O9 (734.60): C, 62.07; H, 4.49; N, 5.72percent. Found: C, 62.03; H, 4.46; N, 5.71percent.
  • 6
  • [ 1135-32-6 ]
  • [ 2991-28-8 ]
  • 2C7H3F3O2*C12H10N2 [ No CAS ]
  • 7
  • copper(II) acetate dihydrate [ No CAS ]
  • [ 32703-79-0 ]
  • [ 1135-32-6 ]
  • [Cu2(1,2-bis(4-pyridyl)ethene)2(tbph)2]n [ No CAS ]
YieldReaction ConditionsOperation in experiment
With potassium hydroxide; In water; at 119.84℃; for 72h;Autoclave; Complex1was prepared according to the methods as follows.A mixture of <strong>[32703-79-0]4-tert-butyl-phthalic anhydride</strong> (40.6 mg,0.2 mmol), Cu(OAc)2¢2H2O (19.1 mg, 0.1 mmol), bpe(36.4 mg, 0.20 mmol), and KOH (11.2 mg, 0.2 mmol) wereadded to water (10 mL) in a 25 mL Teflon-lined autoclave.The mixture was heated at 393 K for three days and thenslowly cooled down to room temperature. Traces of blue blockcrystals of 1 were obtained. Anal. Calcd. (%) forC48H44Cu2N4O8: C, 61.86; H, 4.76; N, 6.01. Found, C, 61.78;H, 4.71; N, 6.08. IR (cm1): 2962 w, 1614 s, 1563 m, 1543 m,1427 m, 1408 m, 1359 m, 1335 s, 1251 m, 1028 m, 835 s,810 m, 789 m, 741 m, 677 m.Complex2 was carried out in a similar way to thatdescribed for1, except that <strong>[32703-79-0]4-tert-butyl-phthalic anhydride</strong>was replaced by H2mph (36.0 mg, 0.2 mmol). Blue block crystals of 2 were obtained. Anal. Calcd. (%) forC36H31CuN3O9: C, 60.63; H, 4.38; N, 5.89. Found: C, 60.54;H, 4.30; N, 5.76. IR (cm1): 3632 w, 2911 w, 1715 m,1608 m, 1532 s, 1506 s, 1402 s, 1373 s, 1302 m, 1223 m,1209 m, 1022 m, 984 m, 969 m, 894 m, 678 s.
  • 8
  • manganese(II) chloride tetrahydrate [ No CAS ]
  • [ 23351-91-9 ]
  • [ 7732-18-5 ]
  • [ 1135-32-6 ]
  • [Mn(5-bromoisophthalate)(1,2-bis(4-pyridyl)ethylene)·1/2H2O]n [ No CAS ]
  • 9
  • cobalt(II) chloride hexahydrate [ No CAS ]
  • [ 23351-91-9 ]
  • [ 7732-18-5 ]
  • [ 1135-32-6 ]
  • [Co(5-bromoisophthalate)(1,2-bis(4-pyridyl)ethylene)1.5·1/2H2O]n [ No CAS ]
  • 10
  • zinc(II) nitrate hexahydrate [ No CAS ]
  • [ 118996-38-6 ]
  • [ 68-12-2 ]
  • [ 1135-32-6 ]
  • 3Zn(2+)*2C21H12NO6(3-)*C12H10N2*C3H7NO*6H2O [ No CAS ]
YieldReaction ConditionsOperation in experiment
at 80.0℃; for 24h;Sealed tube; High pressure; BUT-161: H3TCA (3.8mg, 0.01mmol), DPE (5.5mg, 0.03mmol) and Zn(NO3)2·6H2O (15mg, 0.05mmol) were dissolved in 1mL of anhydrous DMF in a sealed glass vial. The resulting mixture was ultrasonicated to dissolve all the starting materials and then heated at 80C for 24h. After cooling to room temperature, yellow block crystals of as-synthesized BUT-161 were collected by filtration, washed with anhydrous DMF. Anal. Calc. (%) for Zn3C57H53O19N5: C, 52.33; H, 4.08; N, 5.35. Found: C, 51.17; H, 4.21; N, 5.18. FT-IR spectra of ligand H3TCA, DPE and BUT-161a and TGA curves of as-synthesized and activated BUT-161 are shown in Figs. S1 and S2 in supporting information, respectively.
  • 11
  • [ 1071125-59-1 ]
  • [ 1135-32-6 ]
  • C27H18O9*C12H10N2 [ No CAS ]
 

Historical Records

Categories